AU725582B2 - Therapeutic treatment for cardiovascular diseases - Google Patents
Therapeutic treatment for cardiovascular diseases Download PDFInfo
- Publication number
- AU725582B2 AU725582B2 AU34763/97A AU3476397A AU725582B2 AU 725582 B2 AU725582 B2 AU 725582B2 AU 34763/97 A AU34763/97 A AU 34763/97A AU 3476397 A AU3476397 A AU 3476397A AU 725582 B2 AU725582 B2 AU 725582B2
- Authority
- AU
- Australia
- Prior art keywords
- alkyl
- independently
- hydrogen
- alkylene
- protein kinase
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
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Abstract
A method for treating endothelial cell dysfunction, such as associated with cardiovascular disease are disclosed, particularly using the isozyme selective PKC inhibitor, (S)-3,4-[N,N'-1,1'-((27''-ethoxy)-3'''(O)-4'''-(N,N-dimethylamino)-butane)-bis-(3,3'-indolyl)]-1(H)-pyrrole-2,5-dione hydrochloride salt.
Description
WO 97/47298 PCT/US97/09661 THERAPEUTIC TREATMENT FOR CARDIOVASCULAR DISEASES This application is a continuation-in-part of Heath et al., application U.S.
Serial No. 08/643,706 filed May 6, 1996, which is a divisional of Heath et al., U.S.
Serial No. 08/413,735, filed March 30, 1995, which is a continuation-in-part of Heath et al., U.S. Serial No. 08/316,973, filed October 3, 1994, which is a continuation-inpart of Heath et al., U.S. Serial No. 08/163,060, filed December 7, 1993.
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is broadly directed to a method for treating vascular endothelial cell dysfunction, especially dysfunction induced by hyperglycemia. The present invention is particularly directed to the use of a particular class of isozyme selective Protein Kinase C (PKC) inhibitors for treating atherosclerotic disease states especially cardiovascular diseases associated with vascular endothelial cell dysfunction.
2. Description of Related Art Injury or dysfunction of the vascular endothelium is a common feature shared by many conditions that predispose an individual to accelerated development of atherosclerotic cardiovascular disease. One of the most prevalent factors that causes endothelial cell dysfunction is hyperglycemia. Evidence suggests that hyperglycemia S WO 97/47298 PCTUS97/09661 is directly toxic to endothelial cells. Using techniques such as acetylcholine induced vasodilation as an indicator of endothelial cell function, multiple studies have demonstrated that endothelial cell dysfunction is apparent in nonhuman models of diabetes. Several studies in humans have demonstrated that a similar dysfunction of the endothelium exists in humans with diabetes. Although certain types of diabetes are accompanied with other cardiovascular risk factors such as obesity, hypertension and dyslipidemias, these concomitant risk factors do not account for the increased risk of developing the clinical manifestations of atherosclerosis seen in diabetic patients.
Several groups have suggested that the occurrence ofmicroalbuminuria in both diabetic and non-diabetic patients reflects a generalized worsening of their endothelial cell function. In diabetic patients, the onset of microalbuminuria is associated with a large increase in the risk of exhibiting the clinical manifestations of atherosclerotic macrovascular disease that is independent of other conventional cardiovascular risk factors. In non-diabetic populations, the onset of microalbuminuria is associated with an increase in the risk of developing macrovascular atherosclerosis and cardiovascular disease. Thus, the widespread endothelial cell dysfunction associated with the onset of microalbuminuria strongly correlates with a dramatic increase in cardiovascular disease. These findings suggest that vascular endothelial cell dysfunction may be the etiology explaining the increase in cardiovascular disease seen in both diabetic and non-diabetic patients with microalbuminuria. Furthermore, the treatment of microalbuminuria has been associated with a lowering of blood lipids and blood pressure.
In addition to predisposing a patient to chronic complications of a WO 97/47298 PCT/US97/09661 atherosclerosis, vascular endothelial cell dysfunction also is associated with acute sequela of atherosclerosis such as ischemic-reperfusion injury. Both non-diabetic and diabetic patients are at increased risk of sudden death due mainly to cardiovascular causes. Diabetic patients also have an increased mortality rate following a myocardial infarction. The increased mortality rate after a myocardial infarction and the increased incidence of sudden death in diabetic patients can be related to a higher degree of vascular endothelial dysfunction imparted by hyperglycemia in addition to the intrinsic endothelial cell dysfunction associated with ischemia-reperfusion injury.
Populations without overt diabetes, but exhibiting milder elevations in their glucose levels, are also at an increased risk for the development of the clinical manifestations of atherosclerosis, cerebrovascular disease, peripheral vascular disease, myocardial ischemic states, and sudden death. Populations with impaired glucose tolerance have a higher prevalence of atherosclerotic diseases.
Data obtained in several disease demonstrates that predispose to the development of atherosclerosis such as hypertension and hypercholesterolemia are associated with a dysfunctional endothelium and reversal of these factors that predispose the patient to atherosclerosis ameliorates the endothelial cell dysfunction.
Correlating with the improvement in endothelial cell function, seen with reduction of hypercholesterolemia, is a reduction in cardiovascular events. Thus, treatments improving vascular endothelial cell function should reduce the risk of developing clinical manifestations of cardiovascular disease.
Protein kinase C activation occurs during ischemia-reperfusion in nondiabetic animal models and has been implicated in the pathogenesis of myocardial "b WO 97/47298 PCT/US97/09661 injury occurring in the ischemia-reperfusion model. In non-diabetic models of ischemia-reperfusion injury which simulates the pathologic processes occurring during acute myocardial ischemia, endothelial cell dysfunction occurs and is involved in worsening cardiac damage after this injury. Protection against endothelial cell damage in this model reduces myocardial injury after ischemia-reperfusion induced damage.
Given that the ischemia-reperfusion myocardial injury model is thought to reflect the processes occurring during acute myocardial ischemic states, such as myocardial infraction, treatment of non-diabetics patients suffering from acute myocardial ischemia with a PKC inhibitor are expected to exhibit a reduction in myocardial injury and the sequela related to this injury arrhythmia, sudden death, increased infarction size, congestive heart failure, recurrent ischemia, etc.
The ubiquitous nature of the protein kinase C isozymes and their important roles in physiology provide incentives to produce highly selective PKC inhibitors.
Given the evidence demonstrating linkage of certain isozymes to disease states, it is reasonable to assume that inhibitory compounds that are selective to one or two protein kinase C isozymes relative to the other PKC isozymes and other protein kinases are superior therapeutic agents. Such compounds should demonstrate greater efficacy and lower toxicity by virtue of their specificity.
At present, there are limited means to treat vascular endothelial cell dysfunction and the atherosclerotic disease states, especially cardiovascular diseases associated with it. Thus there is a need in the art to employ new therapeutic agents to treat atherosclerotic disease states especially cardiovascular diseases.
14 WO 97/47298 PCT/US97/09661 SUMMARY OF INVENTION It is an object of the invention to provide a method for treating vascular endothelial cell dysfunction.
It is another object of the invention to provide a method for treating cardiovascular disease.
It is yet another object of the invention to provide a method for inhibiting onset of cardiovascular disease.
It is still another object of the invention to provide a method for treating microalbuminuria.
It is another object of the invention to provide a method for treating central ischemia brain injury.
It is yet another object of the invention to provide a method for treating restenosis.
It is still another object of the invention to provide a method for treating atherosclerosis.
It is another object of the invention to provide a method for treating congestive heart failure.
These and other objects of the invention are provided by one or more of the embodiments described below.
In one embodiment of the invention there is provided a method for treating vascular endothelial cell dysfunction which comprises contacting said vascular endothelial cells with a cell dysfunction inhibiting amount of a particular protein kinase C inhibitor.
WO 97/47298 PCT/US97/09661 In another embodiment of the invention there is provided a method for treating cardiovascular disease which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
In still another embodiment of the invention there is provided a method for inhibiting onset of cardiovascular disease in a mammal, which comprises administering to the mammal in need of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
In another embodiment of the invention there is provided a method for treating microalbuminuria which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
In still another embodiment of the invention there is provided a method for treating central ischemia brain injury which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
In yet another embodiment of the invention there is provided a method for treating restenosis which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
In yet another embodiment of the invention there is provided a method for treating atherosclerosis which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
In still another embodiment of the invention there is provided a method for treating congestive heart failure which comprises administering to a mammal in need WO 97/47298 PCT/US9709661 of such treatment, a therapeutically effective amount of a particular protein kinase C inhibitor.
The present invention provides the art with compounds which are prophylactic and effective in treating vascular endothelial cell dysfunction. Consequently, the compounds can be used to treat or inhibit the onset of atherosclerotic disease states, especially cardiovascular diseases associated with vascular endothelial cell dysfunction.
DETAILED DESCRIPTION OF THE INVENTION It is a discovery of the present invention that using a particular class of protein kinase C inhibitors reduces vascular endothelial cell dysfunction associated with atherosclerotic disease states, and in particular the endothelial cell dysfunction induced by hyperglycemia. Consequently, such compounds can be used therapeutically to treat a variety of atherosclerotic disease states especially cardiovascular diseases, and prophylactically to inhibit the development of such diseases.
The method of this invention preferably utilizes the isozyme selective protein kinase C inhibitor compounds of formula I: WO 97/47298 PCT/US97/09661 wherein: W is -SO 2
C
2
-C
6 alkylene, substituted alkylene, C 2
-C
6 alkenylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused bicyclic-, -fused bicyclic-(CH 2
-NR
3
-NOR
3 -CONH-, or -NHCO-; X and Y are independently C,-C 4 alkylene, substituted alkylene, or together X, Y, and W combine to form -(CH 2 n)-AA-; R's are hydrogen or up to four optional substituents independently selected from halo, C,-C 4 alkyl, hydroxy, C-C 4 alkoxy, haloalkyl, nitro, NR 4
R
5 or -NHCO(C-
C
4 alkyl);
R
2 is hydrogen, CH 3 CO-, NH 2 or hydroxy;
R
3 is hydrogen, (CH)aryl, C,-C 4 alkyl, -COO(C,-C 4 alkyl), -CONR 4
R
5 (C=NH)NH2, -SO(C,-C 4 alkyl), -SO2 (NR 4
R
5 or -SO 2
(C-C
4 alkyl);
R
4 and R 5 are independently hydrogen, C,-C 4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring; AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
These compounds, and methods for their preparation, are known and have been disclosed in Heath et al., EP publication 0 657 458 Al which is incorporated herein by reference. These compounds are administered in a therapeutically effective amount, a vascular endothelial cell dysfunction inhibiting amount, to a mammal g WO 97/47298 PCT/US97/09661 to treat endothelial cell dysfunction. The endothelial cell dysfunction can be induced by a variety of factors, hyperglycemia, hypertension, hypercholesterolemia, and ischemic-reperfusion injury.
Such endothelial cell dysfunction can be associated with atherosclerotic disease states including cerebrovascular diseases, central ischemia brain injury, cerebrovascular accidents and transient ischemic attacks; peripheral vascular diseases, nontraumatic amputations and intermittent claudication, and cardiovascular diseases, stable angina, unstable angina, variant angina, sudden death, myocardial infarction, restenosis, and ischemia-reperfusion injury. Consequently, these compounds can be used to treat these various atherosclerotic disease states, especially the cardiovascular diseases discussed above.
The compounds also can be administered in a prophylactically effective amount to patients at risk of developing atherosclerotic disease states, especially cardiovascular diseases, such as patients with hyperglycemia, hypertension, or hypercholesterolemia, as a prophylactic.
The preferred compounds for use in this invention are those of formula I wherein the moieties contain 4 to 8 atoms, which may be substituted or unsubstituted. Most preferably, the moieties contain 6 atoms.
Other preferred compounds for use in this invention are those compounds of formula I wherein R' and R 2 are hydrogen; and W is a substituted alkylene, -CONH-, -NHCO- or -NR 3 Particularly preferred compounds are compounds of the formula la: WO 97/47298 PCT/US97/09661 'N N (la) (C H 2 (CH2)m z Z14
R
wherein Z is -(CH 2 or -(CH 2) p-O-(CH 2) R 4 is hydroxy, -SH, C -C 4 alkyl,
(CH
2 )maryl, -NH(aryl), -N(CH 3
(CF
3
-NH(CF
3 or -NRR 6
R
5 is hydrogen or C,-C4 alky; R 6 is hydrogen, C 1
-C
4 alkyl or benzyl; p is 0, 1, or 2; and m is independently 2 or 3 or a pharmaceutically acceptable sale, prodrug or ester thereof. Most preferred compounds of the formula la are those wherein Z is -CH 2 and R 4 is -NH 2
-NH(CF
3 or -N(CH 3 2 Other preferred compounds for use in the present invention are compounds wherein W in formula I is Y is a substituted alkylene, and X is an alkylene.
These preferred compounds are represented by formula Ib: S(Ib) N N (Ib) WO 97/47298 PCT/US97/09661 wherein Z is -(CH 2
R
4 is -NRR 6 -NH(CF), or -N(CH) R 5 and R 6 are independently H or C,-C 4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof. Most preferred compounds of formula Ib are those wherein p is 1; and R 5 and R 6 are methyl.
Because they contain a basic moiety, the compounds of formula I, la and Ib can also exist as pharmaceutically acceptable acid addition salts. Acids commonly employed to form such salts include inorganic acids such as hydrochloric, hydrobromic, hydroiodic, sulfuric and phosphoric acid, as well as organic acids such as para-toluenesulfonic, methanesulfonic, oxalic, para-bromophenylsulfonic, carbonic, succinic, citric, benzoic, acetic acid, and related inorganic and organic acids. Such pharmaceutically acceptable salts thus include sulfate, pyrosulfate, bisulfate, sulfite, bisulfite, phosphate, mono-hydrogenphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate, propionate, decanoate, caprylate, acrylate, formate, isobutyrate, heptanoate, propiolate, oxalate, malonate, succinate, suberate, sebacate, fumarate, maleate, 2-butyne-l,4-dioate, 3-hexyne-2, benzoate, chlorobenzoate, hydroxybenzoate, methoxybenzoate, phthalate, xylenesulfonate, phenylacetate, phenylpropionate, phenylbutyrate, citrate, lactate, hippurate, P-hydroxybutyrate, glycolate, maleate, tartrate, methanesulfonate, propanesulfonate, naphthalene-1-sulfonate, naphthalene-2-sulfonate, mandelate and the like.
In addition to pharmaceutically-acceptable salts, other salts also can exist.
n WO 97/47298 PCT/US97/09661 They may serve as intermediates in the purification of the compounds, in the preparation of other salts, or in the identification and characterization of the compounds or intermediates.
The pharmaceutically acceptable salts of compounds of formulae I, Ia and Ib can also exist as various solvates, such as with water, methanol, ethanol, dimethylformamide, ethyl acetate and the like. Mixtures of such solvates can also be prepared. The source of such solvate can be from the solvent of crystallization, inherent in the solvent of preparation or crystallization, or adventitious to such solvent.
It is recognized that various stereoisomeric forms of the compounds of formulae I, Ia and Ib may exist; for example, W may contain a chiral carbon atom in the substituted alkylene moiety. The compounds are normally prepared as racemates and can conveniently be used as such. Alternatively, both individual enantiomers can be isolated or synthesized by conventional techniques if so desired. Such racemates and individual enantiomers and mixtures thereof form part of the compounds used in the methods of the present invention.
The compounds utilized in this invention also encompass the pharmaceutically acceptable prodrugs of the compounds of formulae I, Ia and Ib. A prodrug is a drug which has been chemically modified and may be biologically inactive at its site of action, but which may be degraded or modified by one or more enzymatic or other in vivo processes to the parent bioactive form. This prodrug likely may have a different pharmacokinetic profile than the parent, enabling easier absorption across the mucosal epithelium, better salt formation or solubility, and/or improved systemic stability (an
I
WO 97/47298 PCT/US97/09661 increase in plasma half-life, for example). Typically, such chemical modifications include the following: 1) ester or amide derivatives which may be cleaved by esterases or lipases; 2) peptides which may be recognized by specific or nonspecific proteases; or 3) derivatives that accumulate at a site of action through membrane selection of a prodrug form or a modified prodrug form; or any combination of 1 to 3, supra. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in H.
Bundgaard, Design of Prodrugs, (1985).
The synthesis of various bis-indole-N-maleimide derivatives is described in Davis et al. U.S. Patent 5,057,614 and the synthesis of the preferred compounds suitable for use in this invention are described in the previously identified Heath et al.O EP publication 657 458 and in Faul et al. EP publication 0 657 411 Al, both of which are incorporated herein by reference.
One particularly preferred protein kinase C inhibitor for use in the method of this invention is the compound described in Example 5s ethoxy)-3"(0)-4"'-(N,N-dimethylamino)-butane)-bis-(3,3'-indoly )]-1(H)-pyrrole-2,5dione Hydrochloride Salt) of the aforementioned EP publication 0 657 458 Al. This compound is a potent protein kinase C inhibitor. It is selective to protein kinase C over other kinases and is highly isozyme-selective, it is selective for the beta-1 and beta -2 isozymes. This compound is shown to normalize endothelial cell WO 97/47298 PCT/US97/09661 dysfunction in animal models of diabetes at doses predictive to selectively inhibit PKC-p. The data are reported in Hidehiro et al., Science Vol. 272, page 728-731, 1996 and is incorporated herein by reference.
In streptozotocin and alloxan diabetic rodents, this compound normalized changes induced by diabetes in retinal blood flow and vascular Na/K-ATPase activity.
Changes in retinal blood flow reflect hyperglycemic induced abnormalities in endothelial cell regulation of blood flow. Decreases in Na/K-ATPase activity is a indication of abnormal endothelial cell function (Gupta, et al., J. Clin. Invest., 90:727- 732 (1991)). The ability of this compound to normalize these diabetic induced abnormalities demonstrates its protective effect on the endothelium in hyperglycemic states. In addition, this compound blocked microalbuminuria, a marker of widespread endothelial cell dysfunction. Thus, in the rodent model of diabetes, this compound reduces the glucose-mediated endothelial cell toxicity and inhibited the endothelial cell dysfunction that is associated with the development of atherosclerotic macrovascular disease.
Vascular endothelial cell dysfunction is strongly associated with atherosclerotic cardiovascular disease in diabetic and nondiabetic patients. The compounds of this invention, being active for normalizing vascular endothelia cell dysfunctions are particularly useful for treating cardiovascular diseases stable angina, unstable angina, variant angina, cardiovascular ischemia, sudden death, and myocardial infarction, especially the cardiovascular diseases associated with hyperglycemia. In addition to predisposing individuals to chronic complications of atherosclerosis, endothelial cell dysfunction also is associated with acute sequela of \q WO 97/47298 PCT/US97/09661 atherosclerosis such as ischemic-reperfusion injury (Ku, Science, 218:576-578 (1982); Van Benthuysen, et al., J. Clin. Invest., 79:265-274 (1987); Mehta, et al., Cir. Res., 64:43-54 (1989)). The compounds useful in the method of this invention are therapeutically effective for reducing endothelial cell dysfunction occurring after an ischemic episode and on reducing the clinical sequela associated with this abnormality, sudden death and a higher mortality rate after a myocardial infarction.
The compounds of this invention also can be used to reduce the risk of cardiovascular disease seen in persons exhibiting hyperglycemia. A normal range of plasma glucose level is 75 to 105 mg/dl (4.2 to 5.8 mmol per liter) in fasting condition and up to 140 mg/dl (up to 7.8 mmol per liter) two hours postprandial. The compounds thus can be used prophylactively to treat patients where glucose levels are in the upper range of normal and in patients exhibiting impaired glucose tolerance, hypertension, hypercholesterolemia, and diabetes.
Microalbuminuria and macrovascular endothelial cell dysfunction reflect a generalized worsening of vascular endothelial cell function in diabetic and nondiabetic patients. The compounds in the present invention can be used therapeutically to treat these conditions.
The term "treating," as used herein, describes the management and care of a patient for the purpose of combating the disease, condition, or disorder and includes the administration of a compound of present invention to prevent the onset of the symptoms or complications (prophylactic uses), alleviating the symptoms or complications, or eliminating the disease, condition, or disorder.
E)
WO 97/47298 PCT/US97/09661 The term "isozyme selective" means the preferential inhibition of protein kinase C beta-1 or beta-2 isozyme over protein kinase C isozymes, alpha, gamma, delta, epsilon, zeta, and eta. In general, the compounds useful in the invention demonstrate a minimum of a eight fold differential (preferably a ten fold differential) in the dosage required to inhibit PKC beta-1 or beta-2 isozyme and the dosage required for equal inhibition of the alpha protein kinase C isozyme as measured in the PKC assay. The compounds demonstrate this differential across the range of inhibition and are exemplified at the IC 5 0 a 50% inhibition. Thus, isozyme-selective compounds inhibit the beta-1 and beta-2 isozymes of protein kinase C at much lower concentrations with lower toxicity by virtue of their minimal inhibition of the other PKC isozymes.
One skilled in the art will recognize that a therapeutically effective amount, an endothelial cell dysfunction inhibiting amount, of the protein kinase C inhibitor of the present invention is an amount sufficient to inhibit the endothelial cell dysfunction or inhibit development of cardiovascular disease and that this amount varies inter alia, depending upon an affected tissue size, the concentration of the compound in the therapeutic formulation, and the body weight of the patient.
Generally, an amount of protein kinase C inhibitor to be administered as a therapeutic agent for treating cardiovascular disease, and for inhibiting onset of cardiovascular disease as discussed above, will be determined on a case by case basis by the attending physician. As a guideline, the extent of the vascular endothelial cell dysfunctions, the body weight, and age of the patient will be considered when setting an appropriate dose.
WO 97/47298 PCTUS97/09661 Generally, a suitable dose is one that results in a concentration of the protein kinase C inhibitor at the treatment site in the range of 0.5 nM to 200 and more usually 0.5 nM to 200 nM. It is expected that serum concentrations of 0.5 nM to nM should be sufficient in most circumstances.
To obtain these treatment concentrations, a patient in need of treatment likely will be administered between about 0.001 mg per day per kg of body weight and 50.0 mg per day per kg. Usually, not more than about 10.0 mg per day per kg of body weight of protein kinase C inhibitor need be needed. As noted above, the above amounts may vary on a case-by-case basis.
One skilled in the art will also recognize that a prophylactically effective amount of the protein kinase C inhibitor of the present invention is an amount sufficient to inhibit or reduce the risk of onset of cardiovascular disease. This amount varies depending on the degrees of exhibited risk factors. Generally, an amount of protein kinase C inhibitor to be administered as a prophylactic agent for cardiovascular disease will be determined on a case by case basis by the attending physicians. As a guideline, a suitable dose is determined on the dose of the PKC inhibitors used as therapeutic agents. It normally would range from 50% 150% of the therapeutic dosage discussed above.
The compounds of formula I, and the preferred compounds of formulae Ia and Ib, are preferably formulated prior to administration. Suitable pharmaceutical formulations are prepared by known procedures using well known and readily available ingredients. In making the compositions suitable for use in the method of the present invention, the active ingredient will usually be mixed with a carrier, or 9 WO 97/47298 PCT/US97/09661 diluted by a carrier, or enclosed within a carrier which may be in the form of a capsule, sachet, paper or other container. When the carrier serves as a diluent, it may be a solid, semisolid or liquid material which acts as a vehicle, excipient or medium for the active ingredient. Thus, the compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosol (as a solid or in a liquid medium), soft and hard gelatin capsules, suppositories, sterile injectable solutions and sterile packaged powders for either oral or topical application.
Some examples of suitable carriers, excipient, and diluents include lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphates, alginate, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water syrup, methyl cellulose, methyl and propylhydroxybenzoates, talc, magnesium stearate and mineral oil. The formulations can additionally include lubricating agents, wetting agents, emulsifying and suspending agents, preserving agents, sweetening agents or flavoring agents.
The compositions of the invention may be formulated so as to provide quick, sustained or delayed release of the active ingredient after administration to the patient.
The compositions are preferably formulated in a unit dosage form, each dosage containing from about 0.05 mg to about 3 g, more usually about 750 mg of the active ingredient. However, it will be understood that the therapeutic dosage administered will be determined by the physician in the light of the relevant circumstances, including the severity of the condition to be treated, the choice of compound to be administered and the chosen route of administration. Therefore, the above dosage ranges are not intended to limit the scope of the invention in any way. The term "unit WO 97/47298 PCT/US97/09661 dosage form" refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical carrier.
In addition to the above formulations, most of which may be administered orally, the compounds used in the method of the present invention also may be administered topically. Topical formulations include ointments, creams and gels.
Ointments generally are prepared using either an oleaginous base, one consisting of fixed oils or hydrocarbons, such as white petrolatum or mineral oil, or an absorbent base, one consisting of an anhydrous substance or substances which can absorb water, for example anhydrous lanolin. Customarily, following formation of the base, whether oleaginous or absorbent, the active ingredient (compound) is added to an amount affording the desired concentration.
Creams are oil/water emulsions. They consist of an oil phase (internal phase), comprising typically fixed oils, hydrocarbons, and the like, such as waxes, petrolatum, mineral oil, and the like, and an aqueous phase (continuous phase), comprising water and any water-soluble substances, such as added salts. The two phases are stabilized by use of an emulsifying agent, for example, a surface active agent, such as sodium lauryl sulfate; hydrophilic colloids, such as acacia colloidal clays, veegum, and the like. Upon formation of the emulsion, the active ingredient (compound) customarily is added in an amount to achieve the desired concentration.
Gels comprise a base selected from an oleaginous base, water, or an emulsionsuspension base. To the base is added a gelling agent which forms a matrix in the WO 97/47298 PCTUS97/09661 base, increasing its viscosity. Examples of gelling agents are hydroxypropyl cellulose, acrylic acid polymers, and the like. Customarily, the active ingredient (compounds) is added to the formulation at the desired concentration at a point preceding addition of the gelling agent.
The amount of PKC inhibitor compound incorporated into a topical formulation is not critical; the concentration should be within a range sufficient to permit ready application of the formulation to the affected tissue area in an amount which will deliver the desired amount of compound to the desired treatment site.
The customary amount of a topical formulation to be applied to an affected tissue will depend upon an affected tissue size and concentration of compound in the formulation. Generally, the formulation will be applied to the effected tissue in an amount affording from about 1 to about 500 bg compound per cm 2 of an affected tissue. Preferably, the applied amount of compound will range from about 30 to about 300 Mg/cm 2 more preferably, from about 50 to about 200 uzg/cm and, most preferably, from about 60 to about 100 ug/cm 2 The following formulation examples are illustrative only and are not intended to limit the scope of the invention in any way.
Formulation I Hard gelatin capsules are prepared using the following ingredients: Quantity (mg/capsule) Active agent 250 starch, dried 200 magnesium stearate WO 97/47298 PCT/US97/09661 460 mg Total The above ingredients are mixed and filled into hard gelatin capsules in 460 mg quantities.
Formulation 2 A tablet is prepared using the ingredients below: Active agent cellulose, microcrystalline silicon dioxide, fumed stearic acid Quantity (mg/capsule) 250 400 665 mg Total The components are blended and compressed to form tablets each weighing 665 mg.
Formulation 3 Tablets each containing 60 mg of active ingredient are made as follows: Active agent starch microcrystalline cellulose polyvinylpyrrolidone (as 10% solution in water) sodium carboxymethyl starch magnesium stearate talc Quantity (mg/tablet) 60 mg 45 mg 35 mg 4 mg 4.5 mg 0.5 mg 1 mg 150 mg Total WO 97/47298 PCT[US97/09661 The active ingredient, starch and cellulose are passed through a No. 45 mesh U.S. sieve and mixed thoroughly. The solution ofpolyvinylpyrrolidone is mixed with the resultant powders which are then passed through a No. 14 mesh U.S. sieve. The granules so produced are dried at 50°C and passed through a No. 18 mesh U.S. sieve.
The sodium carboxymethyl starch, magnesium stearate and talc, previously passed through a No. 60 mesh U.S. sieve, are then added to the granules which, after mixing, are compressed on a tablet machine to yield tablets each weighing 150 mg.
Formulation 4 Capsules each containing 80 mg of medicament are made as follows: Quantity (mg/capsule) Active agent 80 mg starch 59 mg microcrystalline cellulose 59 mg magnesium stearate 2 mg Total 200 mg The active ingredient, cellulose, starch and magnesium stearate are blended, passed through a No. 45 mesh U.S. sieve, and filled into hard gelatin capsules in 200 mg quantities.
The principles, preferred embodiments and modes of operation of the present invention have been described in the foregoing specification. The invention which is intended to be protected herein, however, is not to be construed as limited to the particular forms disclosed, since they are to be regarded as illustrative rather than restrictive. Variations and changes may be made by those skilled in the art without CD/00370191.5 23 departing from the spirit of the invention.
It will also be understood that the term "comprises" (or its grammatical variants) as used in this specification is equivalent to the term "includes" and should not be taken as excluding the presence of other elements or features.
s
Claims (35)
1. A method for treating vascular endothelial cell dysfunction associated with a condition selected from the group consisting of stable angina, unstable angina, variant angina, sudden death and myocardial infarction in a mammal comprising administering to a mammal in need of such treatment a cell dysfunction inhibiting amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: R 2 (I) R() N N W :wherein: 10 W is -SO2-, C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH2)mO-, -heterocycle-, -heterocycle-(CH2)mO-, -fused bicyclic-, -fused bicyclic-(CH2)mO-, -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR 4 R 5 or -NHCO(C1-C4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 PAi (C=NH)NH 2 -SO(C1-C 4 alkyl), -SO 2 (NR 4 R 5 or -SO 2 (C-C4 alkyl); SR 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or CD/00370191.5 combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
2. A method according to claim 1, wherein the protein kinase C inhibitor has the following formula: H N (la) (la) r e r r (CH 2 )I wherein Z is -(CH 2 or -(CH 2 )p-O-(CH 2 R 4 is hydroxy, -SH, C1-C4 alkyl, (CH 2 )maryl, -NH(aryl), -N(CH 3 (CF 3 -NH(CF 3 or -NR 5 R 6 R 5 is hydrogen or Ci- C4 alkyl; R 6 is hydrogen, C1-C4 alkyl or benzyl; p is 0, 1, or 2; and m is independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof.
3. A method according to claim 1 wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 26 H Sc (Ib) N N (CH 2 )m \o(CH2)m Z 14 qR wherein Z is -(CH 2 R 4 is -NR 5 R 6 -NH(CF 3 or -N(CH 3 (CF 3 R 5 and R 6 are independently H or CI-C4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof. 5 4. A method according to claim 1, wherein the protein kinase C inhibitor °comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)-butane)- bis-(3,3'-indolyl)]-1 (H)-pyrrole-2,5-dione or its acid salt.
5. A method for treating cardiovascular disease associated with a condition selected from the group consisting of stable angina, unstable angina, variant angina and myocardial infarction, which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: I CD/003701 9 1. 27 R 2 1 0 N SR(I) N N I I X Y W wherein S..W is -S02-, C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH2)mO-, -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or -NHCO( C 1 -C 4 alkyl); R is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C-C4 alkyl, -COO(C1-C4 alkyl), -CONR4R, (C=NH)NH 2 -SO(C 1 -C 4 alkyl), -S02 (NR4R 5 or -S02 (C-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
6. A method according to claim 5, wherein the protein kinase C inhibitor CD/00370191 has the following formula: (la) (CH 2 )m (CI-12) S S S wherein Z is -(0H 2 or -(0H 2 )p-O-(0H 2 R 4 is hydroxy, -SH, 01-04 alkyl, (0H 2 )maryl, -NH(aryl), -N(CH 3 (CE 3 -NH(0FA) or -NR 5R 6; R 5 is hydrogen or Cj- 5 C4 alkyl; R 6 is hydrogen, 01-04 alkyl or benzyl; p is 0, 1, or 2; and m is independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof.
7. A method according to claim 5, wherein the protein kinase 0 inhibitor has the following formula: CD/00370191.5 29 H S^ I l b) N N (CH2)m (CH 2 )m z 14 R 4 wherein Z is -(CH 2 R 4 is -NR R 6 -NH(CF 3 or -N(CH 3 (CF3); R s and R 6 are ;independently H or C 1 -C 4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof. 5 8. A method according to claim 5, wherein the protein kinase C inhibitor l.e comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(0)-4"'-(N,N-dimethylamino)-butane)- bis-(3,3'-indolyl)]-1(H)-pyrrole-2,5-dione or its acid salt. e
9. A method for inhibiting onset of endothelial cell dysfunction associated with a condition selected from the group consisting of stable angina, unstable angina, variant angina, sudden death and myocardial infarction in a mammal, which comprises administering to a mammal a prophylactically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 R 2 R- R SO I) N N W wherein: S. W is -S0 2 C2-C6 alkylene, substituted alkylene, C2-C6 :alkylene, -aryl-, -aryl(CH2)mO-, -heterocycle-, -heterocycle-(CH2)mO-, -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or-NHCO(C1-C 4 alkyl); R 2 is hydrogen, CHaCO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C 4 alkyl), -SO2 (NR 4 R 5 or -SO 2 (Ci-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof. R 10. A method according to claim 9, wherein the protein kinase C inhibitor rh as the following formula: CD/003701 91.5 31 H (la) (0H 2 )m (0H 2 )m z 14 R wherein Z is -(0H 2 or -(0H 2 )p-O-(0H 2 R 4 is hydroxy, -SH, 01-04 alkyl, (CH 2 )maryI, -NH(aryl), -N(0H 3 (OF 3 -NH(CF 3 or -NR R R 5 is hydrogen or 0j- 04 alkyl; R 6 is hydrogen, 01-04 alkyl or benzyl; p is 0, 1, or 2; and m is independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof. *11. A method according to claim 9, wherein the protein kinase 0 inhibitor has the following formula: CD/00370191.5 32 H O N 0 C N /O (Ib) N N (CH 2 )m (CH2)m Z 5 R 4 wherein Z is -(CH 2 R 4 is -NR 5 R 6 -NH(CF 3 or -N(CH 3 (CF 3 R 5 and R 6 are independently H or C1-C4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof.
12. A method according to claim 9, wherein the protein kinase C inhibitor comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)-butane)- bis-(3,3'-indolyl)]-1 (H)-pyrrole-2,5-dione or its acid salt.
13. A method for treating microalbuminuria, which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 33 R 2 S I) w N N W wherein: W is -SO 2 C2-C6 alkylene, substituted alkylene, C2-C6 o* alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR R, or -NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(Ci-C4 alkyl), -CONR4R (C=NH)NH 2 -SO(C1-C4 alkyl), -SO2 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
14. A method according to claim 13, wherein the protein kinase C r inhibitor has the following formula: CD/00370 191.5 34 (la) (0H 2 )mI (CH 2 )M z *S 9014 00 0 R 900, a C wherein ZRs-C 2 r-CH)--C 2 is hydroxy, SH,01-4 alkylo ezl s0 ,o ;admi (0H 15.mametho aNHcaryi), to0 (cFa), 1N(0 3 or eei theR 6 p 5 i ro en ora C- indepndntt2or 3 olwnormuparmcuial:cetbeslporgo se 0000a CD/00370191.5 H ON /0 I b N N (CH2)m (CH2)m O- *0 wherein Z is -(CH 2 R 4 is -NR 5 R 6 -NH(CFa), or -N(CH 3 (CF 3 R 5 and R 6 are o t independently H or C1-C4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof.
16. A method according to claim 13, wherein the protein kinase C inhibitor comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)- butane)-bis-(3,3'-indolyl)]-1 (H)-pyrrole-2,5-dione or its acid salt.
17. A method according to any one of claims 13 to 16, wherein microalbuminuria is associated with diabetes.
18. A method for treating central ischemia brain injury, which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 36 R 2 S I) N N I I X w Y W wherein: W is -S0 2 C2-C 6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or-NHCO(C1-C4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(Ci-C4 alkyl), -CONRR, (C=NH)NH 2 -SO(C1-C 4 alkyl), -S02 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
19. A method according to claim 18, wherein the protein kinase C Sinhibitor has the following formula: CD/00370191.5 37 H (la) (CH 2 )m (C0H 2 )m z 14 R wherein Z is -(CH 2 or -(0H 2 )p-O-(CH 2 R 4 is hydroxy, -SH, 01-04 alkyl, (CH 2 )maryl, -NH(aryl), -N(0H 3 (CE 3 -NH(CFA) or -NR 5 R 6 R 5 is hydrogen or Cj- 000: 04 alkyl; R 6 is hydrogen, 01-04 alkyl or benzyl; p is 0, 1, or 2; and mn is 5 independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof. A method according to claim 18, wherein the protein kinase 0 .000 inhibitor has the following formula: CD/00370191.5 (Ib) I ,(CH2)m 9 *r o ft oe wherein Z is -(CH 2 R 4 is -NRsR 6 -NH(CF 3 or -N(CH 3 )(CF 3 R 5 and R 6 are independently H or C1-C4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof.
21. A method according to claim 18, wherein the protein kinase C inhibitor comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)- butane)-bis-(3,3'-indolyl)]-l(H)-pyrrole-2,5-dione or its acid salt.
22. A method for treating cerebrovascular disease or peripheral vascular disease, which comprises administering to a mammal in need of such treatment, a therapeutically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 39 R 2 I o I) 0N N N W wherein: W is -S0 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; SR 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR4R s or-NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR4R 5 S0.0. (C=NH)NH 2 -SO(C1-C 4 alkyl), -SO 2 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
23. A method according to claim 22, wherein the protein kinase C Sinhibitor has the following formula: 00/00370191.5 H (la) (0H 2 )m (0H 2 )M z 14 R wherein Z is -(CH 2 or -(CH 2 )p-O-(0H 2 R 4 is hydroxy, -SH, 01-04 alkyl, (0H 2 )maryl, -NH(aryl), -N(CH 3 (CFA) -NH(0F 3 or -NR R R 5 is hydrogen or Cj- 04 alkyl; R 6 is hydrogen, 01-04 alkyl or benzyl; p is 0, 1, or 2; and m is *5 independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof.
24. A method according to claim 22, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 41 H S b N N (CH 2 )m (CH)m z Z 14 R q wherein Z is -(CH 2 R 4 is -NR5R 6 -NH(CF 3 or -N(CH 3 (CF 3 R 5 and R 6 are i. independently H or C1-C4 alkyl; p is O, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof.
25. A method according to claim 22, wherein the protein kinase C inhibitor comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)- butane)-bis-(3,3'-indolyl)]-1 (H)-pyrrole-2,5-dione or its acid salt.
26. A method for treating congestive heart failure in a mammal comprising administering to a mammal in need of such treatment a therapeutically 10 effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 42 R 2 R R I(I) N N X Y W wherein: W is -S02-, C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or-NHCO(C1-C4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, Ci-C4 alkyl, -COO(Cl-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C 4 alkyl), -SO 2 (NR 4 R 5 or -SO 2 (Ci-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
27. A method according to claim 26, wherein the protein kinase C Ainhibitor has the following formula: CD/00370191.5 43 (la) (CH 2 )mI (CH 2 )m z 14 R wherein Z is -(CH 2 or -(CH 2 )p-O-(CH 2 R 4 is hydroxy, -SH, 01-04 alkyl, ~(0H 2 )maryI, -NH(aryl), -N(0H 3 (OF 3 -NH(CFA) or -NR 5 R 6 R 5 is hydrogen or Cr- 04 alkyl; R 6 is hydrogen, 01-04 alkyl or benzyl; p is 0, 1, or 2; and m is 5 independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof.
28. A method according to claim 26, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 44 H I l b) N N (CH 2 )m (CH2)m z Z R 4 :wherein Z is -(CH 2 R 4 is -NR 5 R 6 -NH(CF 3 or -N(CH 3 (CF 3 R 5 and R 6 are independently H or C1-C4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof.
29. A method according to claim 26, wherein the protein kinase C inhibitor comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)- butane)-bis-(3,3'-indolyl)]-1 (H)-pyrrole-2,5-dione or its acid salt.
30. A method for treating congestive heart failure associated with vascular endothelial cell dysfunction associated with a condition selected from the 10 group consisting of stable angina, unstable angina, variant angina, sudden death and myocardial infarction in a mammal comprising administering to a mammal in need of such treatment a therapeutically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 R 2 11 O N O I c I) R R N N X Y W wherein: W is -SO 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C 4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or-NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(Ci-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C4 alkyl), -SO 2 (NR 4 R 5 or -SO2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof.
31. A method according to claim 30, wherein the protein kinase C i4nhibitor has the following formula: 'Iqihiitorfllwn 00/00370191.5 46 H (la) (0H 2 )mi (0H 2 )m z 14 R wherein Z is -(0H 2 or -(0H 2 )P-O-(CH 2 R 4 is hydroxy, -SH, 01-04 alkyl, 5 6 (0H 2 )maryl, -NH(aryl), -N(0H 3 (OF 3 -NH(0FA) or -NR R R 5 is hydrogen or Cj- 04 lky; 6 ishdoe,0-04 alkyl or benzyl; p is 0, 1, or 2; and m is 5 independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof. U32. A method according to claim 30, wherein the protein kinase 0 inhibitor has the following formula: CD/00370191.5 (Ib) (CH 2 )m S S S *SSS S S wherein Z is -(CH 2 R 4 is -NR 5 R 6 -NH(CF 3 or -N(CH 3 (CF 3 R 5 and R 6 are independently H or C1-C4 alkyl; p is 0, 1, or 2; and m is independently 2 or 3, or a pharmaceutically acceptable salt, prodrug or ester thereof.
33. A method according to claim 30, wherein the protein kinase C inhibitor comprises (S)-3,4-[N,N'-1,1'-((2"-ethoxy)-3"'(O)-4"'-(N,N-dimethylamino)- butane)-bis-(3,3'-indolyl)]-1(H)-pyrrole-2,5-dione or its acid salt.
34. A method for treating congestive heart failure associated with myocardial infarction in a mammal comprising administering to a mammal in need of such treatment a therapeutically effective amount of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: CD/00370191.5 48 R 2 R R(I) N N x W wherein: W is -S02-, C2-C6 alkylene, substituted alkylene, C2-C6 S. alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or-NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, Ci-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C4 alkyl), -S02 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof. A method according to claim 34, wherein the protein kinase C iNnhibitor has the following formula: C01003701 91.5 49 H (la) (0H 2 )mI (CH 2 )M z 14 R wherein Z is -(CH 2 or -(GH 2 )p-O-(0H 2 R 4 is hydroxy, -SH, 01-04 alkyl, 5S6. (0H 2 )maryl, -NH(aryl), -N(0H 3 (OF 3 -NH(CFA) or -NR R R 5 is hydrogen or Cj- 004:04 alkyl; R 6 is hydrogen, 01-04 alkyl or benzyl; p is 0, 1, or 2; and m is 5 independently 2 or 3 or a pharmaceutically acceptable salt, prodrug or ester thereof. A method according to claim 34, wherein the protein kinase C inhibitor has the following formula: see% CD/00370191 H 00 I I inhibitor tl compre lyl pNis, 1,o (2;ethnyd-m'(is4indepndetylain3,o)- i bnebis(3omprindyes (H)3,-pyrro-,-dioetory its acid salt. ietylmio) soe 0 00 0 0S 0 38. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: *Vo CD/00370191.5 51 R 2 O~ N R R N c (I) N N X Y W wherein: W is -S0 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused S 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR 4 R s or -NHCO(C1-C4 alkyl); 2 R is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C 4 alkyl), -S02 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof for the preparation of a medicament for the treatment of vascular endothelial cell dysfunction associated with a condition selected from the group tonsisting of stable angina, unstable angina, variant angina, sudden death and CD/00370191.5 52 myocardial infarction.
39. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: R 2 S I) N N w W 5 wherein: W is -SO 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together 10 X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR 4 R 5 or -NHCO(C 1 -C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C0-C 4 alkyl), -SO 2 (NR 4 R 5 or -SO2 (C1-04 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; ff- m is independently 0, 1, 2, or 3; and CD/00370191.5 53 n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for the treatment of cardiovascular disease associated with a condition selected from the group consisting of stable angina, unstable angina, variant angina and myocardial infarction. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: R 2 11 (I) O'N O N wherein: 10 W is -SO 2 C2-Cs alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH2)mO-, -heterocycle-, -heterocycle-(CH2)mO-, -fused bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR4R 5 or -NHCO(C 1 -C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 I O- (C=NH)NH 2 -SO(C1-C4 alkyl), -S02 (NR 4 R 5 or -S02 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or WN O CD/00370191.5 54 combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for inhibiting the onset of endothelial cell dysfunction associated with a condition selected from the group consisting of stable angina, unstable angina, variant angina, sudden death and myocardial infarction.
41. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: R 2 2 N CI I N x 4 W wherein: W is -SO 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH2)mO-, -fused bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; A2O R 1 and R independently are hydrogen or up to four optional substituents /N ndependently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, CD/00370191.5 NR 4 R 5 or -NHCO(C 1 -C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C 1 -C 4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(Ci-C4 alkyl), -SO2 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for treating microalbuminuria.
42. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: 1 W wherein: W is -S02-, C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together S- X, Y and W combine to form -(CH 2 )n-AA-; CD/00370191.5 56 R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR 4 R 5 or -NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )aryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C4 alkyl), -S02 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for treating central ischemia brain 15 injury.
43. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: R I (I) x Y w wherein: W is -SO 2 C2-C6 alkylene, substituted alkylene, C2-C6 W ,W alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH2)mO-, -fused P lkln, hteoyle(H 2 m- CD/00370191.5 57 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R' and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR 4 R 5 or -NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, C1-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(Ci-C4 alkyl), -S02 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and 15 n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for treating cerebrovascular disease or peripheral vascular disease. a
44. Use of a protein kinase C inhibitor, wherein the protein kinase C 20 inhibitor has the following formula: *2 0 SRR 2 CD/00370191.5 58 wherein: W is -SO 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; R' and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, NR 4 R 5 or -NHCO(C1-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, Cl-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C4 alkyl), -SO2 (NR 4 R 5 or -SO2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or 15 unsaturated 5 or 6 member ring' "AA is an amino acid residue; e o• m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, 9 prodrug or ester thereof; 20 for the preparation of a medicament for treating congestive heart failure.
45. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: 0 CD/00370191.5 59 R 2 I o I) R R N N X W wherein: W is -S0 2 C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused 5 bicyclic-, -fused bicyclic-(CH 2 -NR 3 -NOR 3 -CONH-, or -NHCO-; X and Y are independently C1-C4 alkylene, substituted alkylene, or together X, Y and W combine to form -(CH 2 )n-AA-; S* R 1 and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, 10 NR 4 R 5 or-NHCO(CI-C 4 alkyl); R 2 is hydrogen, CH 3 CO-, NH 2 or hydroxy; R 3 is hydrogen, (CH 2 )maryl, 01-C4 alkyl, -COO(C1-C4 alkyl), -CONR 4 R 5 (C=NH)NH 2 -SO(C1-C 4 alkyl), -SO 2 (NR 4 R 5 or -SO 2 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, C1-C4 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; m is independently 0, 1, 2, or 3; and n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for treating congestive heart failure Lassociated with vascular endothelial cell dysfunction associated with a condition selected from the group consisting of stable angina, unstable angina, variant /0 4 CD/00370191.5 angina, sudden death and myocardial infarction.
46. Use of a protein kinase C inhibitor, wherein the protein kinase C inhibitor has the following formula: R 2 R R N N x Y 9W is -SO2-, C2-C6 alkylene, substituted alkylene, C2-C6 alkylene, -aryl-, -aryl(CH2)mO-, -heterocycle-, -heterocycle-(CH2)mO-, -fused 10 X, Y and W combine to form -(CH2)n-AA-; and R independently are hydrogen or up to four optional substituents independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, or -NHCO(CI-C4 alkyl); R2 is hydrogen, CH3CO-, NH2, or hydroxy; ir: 5 wherein: 1 W is hydrogen-, (CH2-, 2- alkylene substituted alkylene, RR-C alkylene, -aryl-, -aryl(CH 2 -heterocycle-, -heterocycle-(CH 2 -fused (C=NH)NHbicycl -SO(C-C4 alkyl)mO-, (NR 3 -NOR-, -CONH-, orC4 alkyl); R4 and R are independently 4 alkyldrogen, -C4substituted alkphenyle, or together 10 X, Y and W combine to form -(CH 2 )n-AA-; combine to the nitrogen to which they are or upnded to four optional substituentsed or independently selected halo, C1-C4 alkyl, hydroxy, C1-C4 alkoxy, haloalkyl, nitro, unsaturated 5 or 6 member ring' AA is hydran amino acid residue;or hydroxy; R 3 is hydroge, H 2 aryl, or 3; alky, -4 alky), -ONR (C=NH)NH 2 -SO(C 1 -C 4 alkyl), -S02 (NR 4 R 5 or -S02 (C1-C4 alkyl); R 4 and R 5 are independently hydrogen, 01-04 alkyl, phenyl, benzyl, or combine to the nitrogen to which they are bonded to form a saturated or unsaturated 5 or 6 member ring' AA is an amino acid residue; 'y ^m is independently 0, 1, 2, or 3; and CD/00370191.5 61 n is independently 2, 3, 4, or 5 or a pharmaceutically acceptable salt, prodrug or ester thereof; for the preparation of a medicament for treating congestive heart failure associated with myocardial infarction.
47. A method for treating vascular endothelial cell dysfunction according to claim 1, substantially as hereinbefore described with reference to any one of the examples. Eli Lilly and Company By their Registered Patent Attorneys Freehills Carter Smith Beadle 11 August 2000 9 *9*
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US08/662,623 US5723456A (en) | 1993-12-07 | 1996-06-13 | Therapeutic treatment for cardiovascular diseases |
US08/662623 | 1996-06-13 | ||
PCT/US1997/009661 WO1997047298A1 (en) | 1996-06-13 | 1997-06-12 | Therapeutic treatment for cardiovascular diseases |
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AU3476397A AU3476397A (en) | 1998-01-07 |
AU725582B2 true AU725582B2 (en) | 2000-10-12 |
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AU34763/97A Ceased AU725582B2 (en) | 1996-06-13 | 1997-06-12 | Therapeutic treatment for cardiovascular diseases |
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US (1) | US5723456A (en) |
EP (1) | EP0954308B1 (en) |
JP (1) | JP2000512293A (en) |
KR (1) | KR20000016625A (en) |
AT (1) | ATE315933T1 (en) |
AU (1) | AU725582B2 (en) |
BR (1) | BR9709727A (en) |
CA (1) | CA2257693A1 (en) |
CZ (1) | CZ406798A3 (en) |
DE (1) | DE69735134T2 (en) |
EA (1) | EA005035B1 (en) |
ES (1) | ES2255106T3 (en) |
HU (1) | HUP0003679A3 (en) |
IL (1) | IL127524A0 (en) |
NO (1) | NO318193B1 (en) |
NZ (1) | NZ333341A (en) |
PL (1) | PL189253B1 (en) |
UA (1) | UA49025C2 (en) |
WO (1) | WO1997047298A1 (en) |
YU (1) | YU57398A (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6147109A (en) * | 1997-10-14 | 2000-11-14 | The General Hospital Corporation | Upregulation of Type III endothelial cell Nitric Oxide Synthase by HMG-CoA reductase inhibitors |
US6180597B1 (en) * | 1998-03-19 | 2001-01-30 | Brigham And Women's Hospital, Inc. | Upregulation of Type III endothelial cell nitric oxide synthase by rho GTPase function inhibitors |
US6127401A (en) | 1998-06-05 | 2000-10-03 | Cephalon, Inc. | Bridged indenopyrrolocarbazoles |
US6423751B1 (en) | 1998-07-14 | 2002-07-23 | The Brigham And Women's Hospital, Inc. | Upregulation of type III endothelial cell nitric oxide synthase by agents that disrupt actin cytoskeletal organization |
US6303646B1 (en) | 1999-08-09 | 2001-10-16 | Zhimin Lu | Cancer treatment with Gö 6976 |
US20050066381A1 (en) * | 2003-09-19 | 2005-03-24 | Children's Hospital Medical Center | Regulation of cardiac contractility and heart failure propensity |
GB0329667D0 (en) | 2003-12-22 | 2004-01-28 | King S College London | Core 2 GlcNAc-T inhibitor |
US20080182801A1 (en) | 2003-12-22 | 2008-07-31 | Btg International Limited | Core 2 glcnac-t inhibitors |
GB0513881D0 (en) | 2005-07-06 | 2005-08-10 | Btg Int Ltd | Core 2 GLCNAC-T Inhibitors III |
DE102004019413A1 (en) * | 2004-04-19 | 2005-11-24 | Phenos Gmbh | Use of substances (e.g. nucleic acids, proteins and peptides), which restrain/reduce the expression and/or activity of protein kinase C-epsilon for the treatment/prevention of e.g. circulatory and vascular diseases |
CN1274303C (en) * | 2004-07-09 | 2006-09-13 | 吕志民 | Use of compound and its derivatives in preparing medicine for treating cancer |
GB0513888D0 (en) | 2005-07-06 | 2005-08-10 | Btg Int Ltd | Core 2 GLCNAC-T Inhibitors II |
WO2007143119A2 (en) * | 2006-06-01 | 2007-12-13 | The Board Of Trustees Of The Leland Stanford Junior University | Method of preventing progression of hypertension-induced heart failure with pkc peptides |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU7918894A (en) * | 1993-12-07 | 1995-06-15 | Eli Lilly And Company | Protein kinase C inhibitors |
AU5381696A (en) * | 1995-03-30 | 1996-10-16 | Eli Lilly And Company | Synthesis of bis-indolylmaleimides |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0699311B2 (en) * | 1986-11-06 | 1994-12-07 | 旭化成工業株式会社 | Anti-vasoconstrictor and vasorelaxant |
US4785085A (en) * | 1986-11-21 | 1988-11-15 | Bristol-Myers Company | Rebeccamycin analogs |
US4808613A (en) * | 1986-11-21 | 1989-02-28 | Bristol-Myers Company | Rebeccamycin derivative containing pharmaceutical composition |
EP0303697B1 (en) * | 1987-03-09 | 1997-10-01 | Kyowa Hakko Kogyo Co., Ltd. | Derivatives of physiologically active substance k-252 |
JPH07113027B2 (en) * | 1987-12-24 | 1995-12-06 | 協和醗酵工業株式会社 | K-252 derivative |
DE3803620A1 (en) * | 1988-02-06 | 1989-08-17 | Goedecke Ag | INDOLOCARBAZOL DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THE SAME |
US5438050A (en) * | 1988-02-06 | 1995-08-01 | Godecke Aktiengesellschaft | Indolocarbazole derivatives, processes for their preparation and compositions containing them |
SK278989B6 (en) * | 1988-02-10 | 1998-05-06 | F. Hoffmann-La Roche Ag | Substituted pyrroles, their use for producing a drug, and the drug on their base |
MC2096A1 (en) * | 1989-02-23 | 1991-02-15 | Hoffmann La Roche | SUBSTITUTED PYRROLES |
US5380746A (en) * | 1989-05-05 | 1995-01-10 | Goedecke Aktiengesellschaft | Bis-(1H-indol-3-YL)-maleinimide derivatives, processes for the preparation thereof and pharmaceutical compositions containing them |
IL94274A0 (en) * | 1989-05-05 | 1991-03-10 | Goedecke Ag | Maleinimide derivatives,process for the preparation thereof and pharmaceutical compositions containing the same |
DE3914764A1 (en) * | 1989-05-05 | 1990-11-08 | Goedecke Ag | New bis(1H-indol-3-yl) maleinimide derivs. - are inhibitors of protein kinase C for treatment of cardiovascular, CNS and immune system disorders |
DE3924538A1 (en) * | 1989-07-25 | 1991-01-31 | Goedecke Ag | INDOLOCARBAZOL AND THEIR USE |
DE3942296A1 (en) * | 1989-12-21 | 1991-06-27 | Goedecke Ag | INDOLOCARBAZOL DERIVATIVES, METHOD FOR THE PRODUCTION AND USE THEREOF |
DE4005970A1 (en) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | NEW TRISUBSTITUTED MALEINIMIDES, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS |
DE4005969A1 (en) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | NEW TRISUBSTITUTED PYRROLE, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS |
CA2046801C (en) * | 1990-08-07 | 2002-02-26 | Peter D. Davis | Substituted pyrroles |
US5292747A (en) * | 1990-08-07 | 1994-03-08 | Hoffman-La Roche Inc. | Substituted pyrroles |
JPH04187687A (en) * | 1990-11-21 | 1992-07-06 | Fuji Photo Film Co Ltd | Preparation of fluorane compound |
EP0580812A1 (en) * | 1991-04-11 | 1994-02-02 | Schering Corporation | Anti-tumor and anti-psoriatic agents |
GB9123396D0 (en) * | 1991-11-04 | 1991-12-18 | Hoffmann La Roche | A process for the manufacture of substituted maleimides |
US5461146A (en) * | 1992-07-24 | 1995-10-24 | Cephalon, Inc. | Selected protein kinase inhibitors for the treatment of neurological disorders |
WO1994007895A1 (en) * | 1992-09-25 | 1994-04-14 | Schering Corporation | Diindolo compounds and pharmaceutical compositions containing them |
DE4243321A1 (en) * | 1992-12-21 | 1994-06-23 | Goedecke Ag | Amino acid derivatives of heterocycles as PKC inhibitors |
AU678435B2 (en) * | 1993-05-10 | 1997-05-29 | F. Hoffmann-La Roche Ag | Substituted pyrroles |
US5624949A (en) * | 1993-12-07 | 1997-04-29 | Eli Lilly And Company | Protein kinase C inhibitors |
UA54427C2 (en) * | 1996-05-01 | 2003-03-17 | Елі Ліллі Енд Компані | Method for treating eye diseases caused by vascular endotelium growth factor |
-
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- 1997-06-12 WO PCT/US1997/009661 patent/WO1997047298A1/en not_active Application Discontinuation
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- 1997-06-12 AT AT97931034T patent/ATE315933T1/en not_active IP Right Cessation
- 1997-06-12 AU AU34763/97A patent/AU725582B2/en not_active Ceased
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- 1997-06-12 DE DE69735134T patent/DE69735134T2/en not_active Expired - Fee Related
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU7918894A (en) * | 1993-12-07 | 1995-06-15 | Eli Lilly And Company | Protein kinase C inhibitors |
AU5381696A (en) * | 1995-03-30 | 1996-10-16 | Eli Lilly And Company | Synthesis of bis-indolylmaleimides |
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EP0954308A1 (en) | 1999-11-10 |
JP2000512293A (en) | 2000-09-19 |
BR9709727A (en) | 1999-08-10 |
IL127524A0 (en) | 1999-10-28 |
CA2257693A1 (en) | 1997-12-18 |
AU3476397A (en) | 1998-01-07 |
DE69735134D1 (en) | 2006-04-06 |
NO985808L (en) | 1999-02-12 |
KR20000016625A (en) | 2000-03-25 |
ES2255106T3 (en) | 2006-06-16 |
WO1997047298A1 (en) | 1997-12-18 |
EP0954308B1 (en) | 2006-01-18 |
UA49025C2 (en) | 2002-09-16 |
US5723456A (en) | 1998-03-03 |
EA005035B1 (en) | 2004-10-28 |
YU57398A (en) | 2000-10-30 |
NZ333341A (en) | 2000-05-26 |
ATE315933T1 (en) | 2006-02-15 |
DE69735134T2 (en) | 2006-08-17 |
PL330604A1 (en) | 1999-05-24 |
EA199900025A1 (en) | 1999-06-24 |
NO318193B1 (en) | 2005-02-14 |
HUP0003679A3 (en) | 2002-09-30 |
PL189253B1 (en) | 2005-07-29 |
CZ406798A3 (en) | 1999-08-11 |
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NO985808D0 (en) | 1998-12-11 |
HUP0003679A2 (en) | 2001-04-28 |
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